Klinik für Anästhesiologie, Intensivmedizin und Schmerztherapie, Universitätsklinikum Knappschaftskrankenhaus Bochum, 44892 Bochum, Germany.
Center for Artificial Intelligence, Medical Informatics and Data Science, University Hospital Knappschaftskrankenhaus Bochum, 44892 Bochum, Germany.
Int J Mol Sci. 2024 Jan 23;25(3):1400. doi: 10.3390/ijms25031400.
Sepsis is a common life-threatening disease caused by dysregulated immune response and metabolic acidosis which lead to organ failure. An abnormal expression of aquaporins plays an important role in organ failure. Additionally, genetic variants in aquaporins impact on the outcome in sepsis. Thus, we investigated the polymorphism (rs17553719) and expression of aquaporin-3 () and correlated these measurements with the survival of sepsis patients. Accordingly, we collected blood samples on several days (plus clinical data) from 265 sepsis patients who stayed in different ICUs in Germany. Serum plasma, DNA, and RNA were then separated to detect the promotor genotypes of mRNA expression of AQP3 and several cytokines. The results showed that the homozygote CC genotype exhibited a significant decrease in 30-day survival (38.9%) compared to the CT (66.15%) and TT genotypes (76.3%) ( = 0.003). Moreover, mRNA expression was significantly higher and nearly doubled in the CC compared to the CT ( = 0.0044) and TT genotypes ( = 0.018) on the day of study inclusion. This was accompanied by an increased IL-33 concentration in the CC genotype (day 0: = 0.0026 and day 3: = 0.008). In summary, the C allele of the polymorphism (rs17553719) shows an association with increased expression and IL-33 concentration accompanied by decreased survival in patients with sepsis.
脓毒症是一种常见的危及生命的疾病,由免疫反应失调和代谢性酸中毒引起,导致器官衰竭。水通道蛋白的异常表达在器官衰竭中起着重要作用。此外,水通道蛋白的遗传变异影响脓毒症的预后。因此,我们研究了水通道蛋白-3 (AQP3) 的多态性 (rs17553719) 和表达,并将这些测量结果与脓毒症患者的生存情况相关联。为此,我们收集了德国不同 ICU 中 265 名脓毒症患者的几天(加临床数据)的血液样本。然后分离血清血浆、DNA 和 RNA,以检测 AQP3 的启动子基因型和几种细胞因子的 mRNA 表达。结果表明,与 CT (66.15%) 和 TT (76.3%) 基因型相比,纯合子 CC 基因型的 30 天生存率显著降低(38.9%)(=0.003)。此外,与 CT ( = 0.0044) 和 TT ( = 0.018) 基因型相比,CC 基因型在纳入研究当天的 mRNA 表达显著升高,几乎翻了一番。这伴随着 CC 基因型中 IL-33 浓度的增加(第 0 天:=0.0026,第 3 天:=0.008)。总之,多态性 (rs17553719) 的 C 等位基因与脓毒症患者中 表达增加和 IL-33 浓度增加以及生存率降低有关。